Tambucci Renato, Thapar Nikhil, Saliakellis Efstratios, Pescarin Matilde, Quitadamo Paolo, Cristofori Fernanda, Lindley Keith J, Borrelli Osvaldo
Neurogastroenterology and Motility Division, Department of Gastroenterology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
J Pediatr Gastroenterol Nutr. 2015 Jun;60(6):776-82. doi: 10.1097/MPG.0000000000000709.
The clinical relevance of esophageal baseline impedance (BI) remains to be determined. In the present study, we explored the impact of gastroesophageal reflux disease (GERD) and esophageal dysmotility on BI.
A total of 18 children with esophageal atresia, 26 children with GERD, and 17 controls prospectively underwent esophagogastroduodenoscopy and pH-impedance monitoring. BI was measured in both proximal and distal esophagus. Gastroesophageal reflux (GER) and bolus transit indicators were defined according to published criteria.
Patients with esophageal atresia showed significantly lower proximal and distal BI values (952 [716-1811] Ω; 895 [284-1189] Ω; respectively) compared with those with GERD (3015 [2368-3975] Ω; 2231 [1770-3032] Ω, P < 0.001 and <0.001, respectively) and controls (3699 [3194-4358] Ω; 3522 [2927-3994] Ω, P < 0.001 and <0.001, respectively). Using linear regression, proximal BI strongly correlated with total bolus transit time (r(2) = 0.61, P < 0.001) and bolus presence time (BPT; r(2) = 0.63, P < 0.001). Distal BI weakly correlated with acid exposure time (r(2) = 0.16, P < 0.01) and longstanding reflux episodes (r(2) = 0.17, P < 0.01), and strongly correlated with total bolus transit time (r(2) = 0.53, P < 0.001) and BPT (r(2) = 0.58, P < 0.001). By logistic regression, BPT predicted low proximal BI values (odds ratio [OR] 1.052; P < 0.05), whereas both GER indicators (acid exposure time: OR 1.56, P < 0.05; longstanding reflux episodes: OR 2.8, P < 0.05) and BPT (OR 1.66, P < 0.01) predicted low distal BI values.
Along the length of esophagus, both bolus transit variables and GER significantly affect BI. This suggests that BI may merely mirror phenomena occurring within the esophageal lumen or wall, limiting its value as a discrete clinical entity to replace variables already used for assessing both GERD and esophageal dysmotility.
食管基线阻抗(BI)的临床相关性仍有待确定。在本研究中,我们探讨了胃食管反流病(GERD)和食管动力障碍对BI的影响。
共有18例食管闭锁患儿、26例GERD患儿和17例对照者前瞻性地接受了食管胃十二指肠镜检查和pH-阻抗监测。在食管近端和远端测量BI。根据已发表的标准定义胃食管反流(GER)和食团通过指标。
与GERD患儿(近端:3015[2368 - 3975]Ω;远端:2231[1770 - 3032]Ω,P均<0.001)和对照者(近端:3699[3194 - 4358]Ω;远端:3522[2927 - 3994]Ω,P均<0.001)相比,食管闭锁患儿的近端和远端BI值显著更低(分别为952[716 - 1811]Ω;895[284 - 1189]Ω)。通过线性回归分析,近端BI与食团总通过时间(r² = 0.61,P < 0.001)和食团存在时间(BPT;r² = 0.63,P < 0.001)密切相关。远端BI与酸暴露时间(r² = 0.16,P < 0.01)和长期反流发作(r² = 0.17,P < 0.01)弱相关,与食团总通过时间(r² = 0.53,P < 0.001)和BPT(r² = 0.58,P < 0.001)密切相关。通过逻辑回归分析,BPT可预测近端BI值较低(比值比[OR]1.052;P < 0.05),而GER指标(酸暴露时间:OR 1.56,P < 0.05;长期反流发作:OR 2.8,P < 0.05)和BPT(OR 1.66,P < 0.01)均可预测远端BI值较低。
在食管全长范围内,食团通过变量和GER均对BI有显著影响。这表明BI可能仅仅反映了食管腔内或管壁内发生的现象,限制了其作为一个独立临床实体来替代已用于评估GERD和食管动力障碍的变量的价值。